Dehydrogenase

ADC Related

ADC Antibody ADC Cytotoxin ADC Linker ADCs Drug-Linker Conjugates for ADC
Angiogenesis

5-alpha Reductase ALK Bcr-Abl BTK EGFR FAK FLT3 HER-2 HIF Src Syk VDA VEGFR
Anti-infection

Antibiotic Arenavirus Bacterial CMV EBV Enterovirus Filovirus Fungal Gli HBV HCV HCV Protease HIV HSV Influenza Virus Parasite RABV Reverse Transcriptase RSV SARS-CoV TMV Virus Protease
Apoptosis

Apoptosis ASK Bcl-2 Caspase c-Myc c-RET Cytohesin DAPK Ferroptosis FKBP IAP Mdm2 p53 PD-1 PD-L1 PERK PKD Ras RIP kinase ROS Survivin Thymidylate Synthase TNF Receptor TNFa TRADD
Autophagy

Autophagy LRRK2 Mitophagy OGA ULK
Cell Cycle

Antifolate APC Aurora Kinase BMI-1 CDK Chk c-Myc Eukaryotic Initiation Factor G-quadruplex HDAC HSP Kinesin LIMK Mad2 Microtubule(Tubulin) Mps1 Nucleoside Antimetabolite/Analog Nur77 p21 PAK PERK PFKFB PLK PPAR Ras Rho ROCK SRPK TOPK Topoisomerase Wee1
Cytoskeletal Signaling

Arp2 3 Complex Bcr-Abl Cardiac Myosin Dynamin Gap Junction Protein HSP Integrin Kinesin Microtubule Associated MLCK Myosin PAK TACC3 Wntbeta-catenin
DNA Damage

ATM(ATR) CRISPR(Cas9) DNA alkylator DNA Stain DNA(RNA) Synthesis GAK HDAC HSP Nucleoside Antimetabolite(Analog) OGG1 p97 PARG PARP RAD51 RNR Sirtuin SMN Telomerase Topoisomerase
Endocrinology & Hormones

5-alpha Reductase ACE Adrenergic Receptor Androgen Receptor Aromatase Estrogenprogestogen Receptor Glucocorticoid Receptor GPR Mineralocorticoid Receptor RAAS THR TSH Receptor
Epigenetics

AMPK Aurora Kinase DNA Methyltransferase Epigenetic Reader Domain EZH1 2 HDAC HIF Histone Acetyltransferase Histone Demethylase Histone Methyltransferase JAK MAT MicroRNA MLL Pim PKC Protein Arginine Deiminase Sirtuin Small Interfering RNA (siRNA) SMYD

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Dehydrogenase

Dehydrogenase related products

Cat No.	Product Name	CAS No.	Product Description
V3885	Ivosidenib (AG-120) racemate	1448346-63-1	Ivosidenib racemate (AG120; RG120; AG-120; RG-120;Tibsovo), the racemic mixture ofIvosidenib, is an orally bioavailable andsmall moleculeIDH1 inhibitor that inhibits mutated cytosolic isocitrate dehydrogenase 1 (IDH1).
V0856	MK-8245	1030612-90-8	MK-8245 (MK8245; MK 8245) is a novel and potentliver-targeted inhibitor of stearoyl-CoA desaturase (SCD) with anti-diabetic and anti-dyslipidemic activities.
V124938	3-(2',5'-Disulfophenylimino)-3H-phenothiazine sodium	1419158-69-2	3-(2',5'-Disulfophenylimino)-3H-phenothiazine sodium is an electron transfer mediator.
V3151	3-Methylpyrazole	1453-58-3	3-Methylpyrazole (also known as 3-MP) is a weak inhibitor ofalcohol dehydrogenase,which are a group of dehydrogenase enzymes that occur in many organisms and facilitate the interconversion between alcohols and aldehydes or ketones with the reduction of nicotinamide adenine dinucleotide (NAD+ to NADH).
V128171	AChE-IN-85		AChE-IN-85 is an acetylcholinesterase inhibitor with an IC50 value of 0.083 μM.
V0855	AGI-5198	1355326-35-0	AGI-5198 (also know as IDH-C35; IDHC35; AGI-5198; AGI 5198) is a novel, highly potent and selective inhibitor of IDH1 (isocitrate dehydrogenase 1) R132H/R132C mutants with potential anticancer activity.
V0862	AGI-6780	1432660-47-3	AGI-6780 (AGI6780; AGI 6780) is a potent and selective inhibitor oftumor-associated mutant IDH2 (isocitrate dehydrogenases 2) R140Q with potential anti-inflammatory activity.
V128917	Antibacterial agent 325		Antibacterial agent 325 is an antibacterial agent.
V128922	Antibacterial agent 330	3031427-16-1	Antibacterial agent 330 is an antibacterial agent.
V11730	ASP9521	1126084-37-4	ASP9521 is a novel, selective, orally bioavailable inhibitor of 17β-hydroxysteroid dehydrogenase type 5 (17βHSD5; AKR1C3).
V4174	BAY-1436032	1803274-65-8	BAY-1436032 is a novel and potent pan-mutant isocitrate dehydrogenase 1 (IDH1) inhibitor both in vitro and in vivo.
V16006	BVT-2733	376640-41-4	BVT-2733 is a selective 11β-hydroxysteroid dehydrogenase type 1 (11β-HSD1) inhibitor, which attenuates obesity and inflammation in diet-induced obese mice.
V18887	CVT-10216	1005334-57-5	CVT-10216, an isoflavone compound, is a novel, highly potent and selective, reversible inhibitor of aldehyde dehydrogenase 2 (ALDH2) with IC50s of 29 and 1300 nM for ALDH2 and ALDH1, respectively.
V39998	DHODH-IN-11	1263303-95-2	DHODH-IN-11 (Compound 14b) is a Leflunomide analogue and a weak inhibitor of dihydroorotate dehydrogenase (DHODH) with a pKa of 5.03.
V133650	DHODH-IN-28		DHODH-IN-28 is a potent fluorescent inhibitor that targets human dihydroorotate dehydrogenase (hDHODH) with an IC50 value of 170 nM.
V134380	DSM1465	3109381-06-5	DSM1465 is a potent and selective inhibitor of Plasmodium falciparum dihydroorotate dehydrogenase (PfDHODH) with an IC50 value of 15 nM and an EC50 value of 1.4 nM against Plasmodium falciparum 3D7 (Pf3D7) parasite.
V136119	Flubeneteram	1676101-39-5	Flubeneteram is a succinate dehydrogenase inhibitor with an IC50 value of 0.0484 μM.
V138128	Isofetamid	875915-78-9	Isofetamid is a succinate dehydrogenase inhibitor and bactericide.
V139549	MDH2-IN-2	3047410-41-0	MDH2-IN-2 is an orally effective MDH2 inhibitor with an IC50 value of 5.9 μM.
V139594	MEDS700	2770979-81-0	MEDS700 is a blood-brain barrier-permeable human dihydroorotate dehydrogenase (hDHODH) inhibitor with an IC50 value of 1.5 nM.